Canonical Allele Identifier: CA2120136022

Gene: F7

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113114137T= , CM000675.2:g.113114137T=	GRCh38
NC_000013.10:g.113768451T= , CM000675.1:g.113768451T=	GRCh37
NC_000013.9:g.112816452T=	NCBI36
NG_009262.1:g.13347T= , LRG_554:g.13347T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.364+177T= MANE Select	ENSP00000329546.4:n.364+177T=
ENST00000346342.7:c.364+177T=	ENSP00000329546.3:n.364+177T=
ENST00000375581.3:c.430+177T=	ENSP00000364731.3:n.430+177T=
ENST00000444337.1:c.*172+177T=	ENSP00000387669.1:n.*172+177T=
ENST00000473085.1:n.311+177T=
ENST00000479674.1:n.697+177T=
ENST00000541084.5:c.178+177T=	ENSP00000442051.2:n.178+177T=
NM_000131.4:c.430+177T= , LRG_554t1:c.430+177T=	NP_000122.1:n.430+177T=
NM_001267554.1:c.178+177T=	NP_001254483.1:n.178+177T=
NM_019616.3:c.364+177T= , LRG_554t2:c.364+177T=	NP_062562.1:n.364+177T=
NR_051961.1:n.451+177T=
XM_006719963.2:c.364+177T=	XP_006720026.1:n.364+177T=
XM_011537474.1:c.364+177T=	XP_011535776.1:n.364+177T=
XM_011537475.1:c.178+177T=	XP_011535777.1:n.178+177T=
XM_011537477.1:c.325+177T=	XP_011535779.1:n.325+177T=
XM_006719963.3:c.409+177T=	XP_006720026.2:n.409+177T=
XM_011537474.2:c.409+177T=	XP_011535776.2:n.409+177T=
XM_011537475.2:c.223+177T=	XP_011535777.2:n.223+177T=
XM_011537476.2:c.-632T=	XP_011535778.1:n.-632T=
NM_019616.4:c.364+177T= MANE Select	NP_062562.1:n.364+177T=
NR_051961.2:n.448+177T=
NM_001267554.2:c.178+177T=	NP_001254483.1:n.178+177T=